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Terminated Phase 2 Interventional

Phase 2 Study of SAR444656 in Adult Participants With Moderate to Severe Atopic Dermatitis

ClinicalTrials.gov ID: NCT06058156

Public ClinicalTrials.gov record NCT06058156. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 7:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multinational, Multicenter, Double-blind, Placebo-controlled Phase 2 Study to Evaluate Efficacy and Safety of SAR444656 in Adult Participants With Moderate to Severe Atopic Dermatitis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multinational, multicenter, double-blind, placebo-controlled, parallel-group Phase 2, 4-arm study in adult participants with moderate to severe AD who are inadequately controlled with topical therapies or for whom such topical therapies are inadvisable and who are candidates for systemic therapy. Participants will be randomized to receive SAR444656 dose 1, dose 2, dose 3 or matching placebo. Participants who meet inclusion/exclusion criteria will be stratified for randomization by severity of AD (moderate \[baseline EASI score \<22\] versus severe \[baseline EASI score ≥22\]). The total duration of study is approximately 24 weeks, including 1 to 4 weeks for screening, 16 weeks for double-blind study treatment and 4 weeks for follow-up.

Study identification

NCT ID
NCT06058156
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sanofi
Industry
Enrollment
70 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 8, 2023
Primary completion
Oct 22, 2025
Completion
Nov 19, 2025
Last update posted
Dec 10, 2025

2023 – 2025

United States locations

U.S. sites
10
U.S. states
5
U.S. cities
9
Facility City State ZIP Site status
Clear Dermatology & Aesthetics Center- Site Number : 8400003 Scottsdale Arizona 85255
Encore Medical Research of Boynton Beach- Site Number : 8400002 Boynton Beach Florida 33436
Revival Research - Doral- Site Number : 8400007 Doral Florida 33122
Encore Medical Research - 6600 Taft St- Site Number : 8400004 Hollywood Florida 33024
Sullivan Dermatology- Site Number : 8400001 Miami Florida 33162
ARA Professionals- Site Number : 8400017 Miami Florida 33176-1032
Encore Medical Research - Weston- Site Number : 8400008 Weston Florida 33331
Wayne Health - Dearborn- Site Number : 8400009 Dearborn Michigan 48126
UPMC Montefiore- Site Number : 8400006 Pittsburgh Pennsylvania 15213
ACRC Trials - Carrollton - Hunt - PPDS- Site Number : 8400012 Carrollton Texas 75010-4632

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 27 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06058156, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 10, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06058156 live on ClinicalTrials.gov.

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